The sequential development of antiglomerular basement membrane nephritis and myeloperoxidase-antineutrophil cytoplasmic antibody-associated vasculitis

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Abstract

A 55-year-old woman presented with deafness, increased levels of myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA), and renal insufficiency with proteinuria and hematuria. Renal biopsy revealed crescentic glomerulonephritis with the linear deposition of immunoglobulin G along the glomerular basement membrane (GBM) and peritubular capillaritis. The anti-GBM antibody levels on admission and 10 days after admission were 11.7 U/mL and 127 U/mL, respectively. These results indicated the sequential development of anti-GBM nephritis and MPO-ANCA-associated vasculitis. This report shows that anti-GBM nephritis may be caused by MPO-ANCA-associated vasculitis because of preceding otitis media, the sequential anti-GBM antibody titers, and the findings of peritubular capillaritis.

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Ohashi, N., Namikawa, A., Ono, M., Iwakura, T., Isobe, S., Tsuji, T., … Yasuda, H. (2017). The sequential development of antiglomerular basement membrane nephritis and myeloperoxidase-antineutrophil cytoplasmic antibody-associated vasculitis. Internal Medicine, 56(19), 2617–2621. https://doi.org/10.2169/internalmedicine.8757-16

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